结晶度
卤素
配体(生物化学)
超分子化学
卤键
材料科学
催化作用
组合化学
纳米技术
金属有机骨架
有机合成
化学
有机化学
分子
烷基
受体
复合材料
吸附
生物化学
作者
Jiahao Zhao,Ning Xia,Zhen‐Nan Tian,Fei Xie,Hongqiang Dong,Guanfei Gong,Xuguan Bai,Jike Wang,Lu Wang,Shigui Chen
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-01-03
卷期号:6 (2): 508-516
被引量:4
标识
DOI:10.1021/acsmaterialslett.3c01276
摘要
The development of diverse linking methods in organic framework materials is crucial for advancing materials science and engineering. The [N-X+-N] halogen bonds are a powerful tool for constructing supramolecular aggregates, including halogen-bonded organic frameworks (XOFs), which have emerged as a new class of organic frameworks. However, the existing production of XOFs often yields insoluble AgI byproducts, impeding XOF crystallinity, performance, and functionality. Hence, alternative methods for XOF preparation are required. Here, we present a novel approach to constructing 2D XOFs via reversible ligand exchange reactions, avoiding unwanted AgI byproducts and enhancing crystallinity. Notably, this approach successfully yields highly crystalline XOF-TPTE, which was unattainable with the previous method. XOF-TPTE exhibits exceptional catalytic activity and recyclability upon Pd(II) loading, showing remarkable selective performance in Heck coupling reactions and indicating its potential for diverse applications. This method broadens XOF construction horizons and expands their preparation and applications.
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